chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	126981235	126981236	T	C	22	GENIC	homozygous	108926736
1	126982489	126982490	C	G	37	GENIC	homozygous	120569323
1	126982493	126982494	C	T	36	GENIC	homozygous	120569325
1	126984312	126984313	A	G	36	GENIC	homozygous	108222187
1	126984389	126984390	T	A	18	GENIC	homozygous	120569327
1	126984496	126984497	A	C	26	GENIC	homozygous	120569330
1	126984499	126984500	G	A	26	GENIC	homozygous	108222189
1	126984615	126984616	C	T	34	GENIC	homozygous	108222191
1	126984872	126984873	T	C	31	GENIC	homozygous	108222193
1	126985223	126985224	C	T	24	GENIC	homozygous	108222195
1	126985383	126985384	T	C	19	GENIC	homozygous	108222197
1	126985480	126985481	A	G	30	GENIC	homozygous	108222199
1	126985509	126985510	G	A	29	GENIC	homozygous	120569332
1	126985533	126985534	T	C	29	GENIC	homozygous	108222201
1	126985672	126985673	C	T	30	GENIC	homozygous	108222203
1	126985704	126985705	C	T	32	GENIC	homozygous	108222205
1	126985813	126985814	T	C	32	GENIC	homozygous	108222206
1	126986077	126986078	G	A	34	GENIC	homozygous	108222208
1	126986088	126986089	C	G	37	GENIC	homozygous	108222210
1	126986148	126986149	T	C	34	GENIC	homozygous	108222212
1	126986962	126986963	C	T	23	GENIC	homozygous	108222218
1	126987362	126987363	A	G	13	GENIC	homozygous	108222222